WO2003082014A1 - Disinfection of instruments - Google Patents
Disinfection of instruments Download PDFInfo
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- WO2003082014A1 WO2003082014A1 PCT/EP2003/003065 EP0303065W WO03082014A1 WO 2003082014 A1 WO2003082014 A1 WO 2003082014A1 EP 0303065 W EP0303065 W EP 0303065W WO 03082014 A1 WO03082014 A1 WO 03082014A1
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- disinfectant
- peroxide
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- acylating agent
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/16—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
- A61L2/18—Liquid substances or solutions comprising solids or dissolved gases
- A61L2/186—Peroxide solutions
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/12—Powders or granules
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group, wherein Cn means a carbon skeleton not containing a ring; Thio analogues thereof
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/14—Boron; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/16—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
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- A61L2103/15—
Definitions
- the present invention relates to a powdery disinfectant comprising a peroxide, an acylating agent and nonionic surfactants and the use of such disinfectants for surface and instrument disinfection, in particular in the field of medicine.
- the object of the present invention was therefore to provide a sufficient disinfectant concentration within a short time and to keep the risk of residues in the system and on the surfaces low.
- the present invention relates to a powdery disinfectant based on active oxygen, containing a peracetic acid-generating system consisting of a peroxide and an acylating agent together with nonionic surfactants.
- nonionic surfactants mentioned are preferably free from alkoxylated alkylphenols and include straight-chain or ether alcohols of the formula which are methyl-branched in the 2-position
- Said peroxide is preferably selected from the group sodium perborate monohydrate, sodium perborate tetrahydrate, sodium percarbonate and mixtures thereof.
- the acylating agent mentioned is preferably selected from the group tetraacetylglycoluril, tetraacetylethylenediamine, diacetylhexahydrotriazinedione and mixtures thereof.
- N-acyl compounds can also be used, which have also been described in the field of detergent chemistry as so-called bleach activators for reaction with hydrogen peroxide in alkaline washing liquors.
- Suitable N-acyl compounds are in particular those which have a further keto group on the nitrogen which carries the acyl group and / or in which the nitrogen is part of a heterocyclic ring system.
- N-acyl compounds are the multiply acylated alkylenediamines, such as tetraacetylethylenediamine, acylated glycolurils, primarily tetraacetylglycoluril, N-acylated hydantoins, hydrazides, triazoles, triazines, urazoles, diketopiperazines, sulfurylamides, lactams and cyanurates.
- acylated alkylenediamines such as tetraacetylethylenediamine, acylated glycolurils, primarily tetraacetylglycoluril, N-acylated hydantoins, hydrazides, triazoles, triazines, urazoles, diketopiperazines, sulfurylamides, lactams and cyanurates.
- the disinfectant according to the invention preferably contains
- Alkalizing agents, complexing agents for water hardness, complexing agents for heavy metal ions and water-soluble inorganic salts, corrosion inhibitors and other surfactants are also suitable as auxiliary agents.
- the amount of such auxiliaries in the preparations can vary within very wide limits, depending on the intended effect. It is usually not more than about 3% by weight, preferably between about 0.001 and about 1% by weight, based on the overall preparation
- Sodium triphosphate is to be mentioned primarily as a complexing agent for the water hardness, but other polyphosphates, salts of nitrilotriacetic acid and salts of organic polycarboxylic acids, for example citric acid, or of polymeric polycarboxylic acids, for example acrylic acid / maleic acid copolymers, are also suitable for this purpose.
- Sodium triphosphate which also acts as an alkalizing agent, is particularly preferred.
- Suitable complexing agents for heavy metal ions which have a decomposing effect on peroxidic compounds, are primarily aminopolycarboxylic acids or their salts, for example ethylenediaminetetraacetic acid, but in particular aminopolyphosphonic acids, such as ethylenediaminetetramethylenephosphonic acid, or else hydroxyethane diphosphonic acid or salts thereof.
- Water-soluble salts can take on the function of fillers or builders, such as sodium sulfate, provided that they do not simultaneously have an alkalizing effect, such as sodium carbonate and sodium silicate.
- Corrosion inhibitors which should be mentioned are, in particular, alkylphosphonic acids, of which octanephosphonic acid is particularly preferred. Dyes, perfume and solubilizing additives should be mentioned as further possible auxiliaries. When used, the disinfectant is usually diluted with water.
- It is preferably dissolved in water in an amount of 1 to 10% by weight.
- the disinfectant according to the invention it is preferred to use the disinfectant according to the invention to kill gram-positive bacteria and / or to kill mycobacteria and / or to kill viruses.
- Corrosion inhibitors, complexing agents and other inorganic salts were used as the remainder to 100% by weight.
- Dehydol 980 is a 2-position methyl branched ether alcohol of the formula
- the virological test results also show an advantage.
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Abstract
Description
„Instrumentendesinfektion" "Instrument disinfection"
Die vorliegende Erfindung betrifft ein pulverförmiges Desinfektionsmittel, umfassend ein Peroxid, ein Acylierungsmittel und nichtionische Tenside und die Verwendung derartiger Desinfektionsmittel zur Oberflächen- und Instrumentendesinfektion, insbesondere auf dem Gebiet der Medizin.The present invention relates to a powdery disinfectant comprising a peroxide, an acylating agent and nonionic surfactants and the use of such disinfectants for surface and instrument disinfection, in particular in the field of medicine.
Zur chemischen Desinfektion von Instrumenten mit Hilfe wäßriger Zubereitungen sind im Laufe der Zeit zahlreiche Vorschläge gemacht worden, in denen die unterschiedlichsten antimikrobiellen Wirkstoffe für die Desinfektion vorgesehen werden. In der Praxis haben Zubereitungen auf Basis von Aldehyden die weiteste Verbreitung gefunden, doch sind auch Präparate mit quartären Ammoniumverbindungen, Phenolen, Alkoholen und anderenFor the chemical disinfection of instruments with the aid of aqueous preparations, numerous proposals have been made in the course of time in which the most varied antimicrobial agents are provided for disinfection. In practice, preparations based on aldehydes have found widespread use, but also preparations containing quaternary ammonium compounds, phenols, alcohols and others
Desinfektionswirkstoffen in Gebrauch. Zubereitungen auf Basis peroxidischer Wirkstoffe, insbesondere von Peressigsäure haben dagegen für diese Anwendung nur geringe Bedeutung erlangt. Ein wesentlicher Grund liegt in der geringen Lagerstabilität derartiger wäßriger Zubereitungen. Wegen der breiten antimikrobiellen Wirksamkeit der Peroxide hat es nicht an Versuchen gefehlt, den Nachteil der geringen Lagerstabilität zu überwinden. So ist beispielsweise in den deutschen Offenlegungsschriften 26 55 599 und 28 15 400 vorgeschlagen worden, die für die Desinfektion benötigten wäßrigen Zubereitungen erst kurz vor Gebrauch aus stabileren Vorstufen, nämlich aus Natriumperborat und Säureanhydriden, herzustellen. Gemäß der deutschen Offenlegungsschrift 27 01 133 werden die wäßrigen Zubereitungen aus Wasserstoffperoxid-Abspaltern und aromatischen Acyloxycarbonsäuren erhalten. Nur wenige dieser Verbindungen liefern aber Desinfektionslösungen mit ausreichend breiter Wirksamkeit, und die Lagerung dieser Acylierungsmittel im Gemisch mit den nötigen anorganischen Peroxiden ist wegen Zersetzungsreaktionen auch nur begrenzte Zeit möglich. Unter der Bezeichnung Sekusept Pulver ist ein Produkt im Handel, bei dessen Auflösung in Wasser durch Umsetzung von Natriumperborat mit Tetraacetylethy- lendiamin (TAED) eine desinfektionswirksame Zubereitung entsteht. Dieses Produkt auf Basis einer N-Acylverbindung besitzt ein breites Wirkungsspektrum und ist lagerstabil. Obwohl auf diese Weise bereits ein hoher Standard bei der Desinfektion von medizinischen Instrumenten erreicht worden ist, wurde weiter an der Verbesserung der peroxidischen Systeme gearbeitet, um noch bestehende Wirkungslücken und Nachteile im Gebrauch zu beseitigen. Insbesondere besteht ein Nachteil derartiger pulvriger Systeme darin, daß sie sich in Wasser nur sehr langsam lösen. Dadurch ergibt sich einerseits der Nachteil, daß die gewünschte Desinfektionsmittelkonzentration erst sehr spät voll zur Verfügung steht. Andererseits besteht zusätzlich das Risiko, daß ungelöste Bestandteile im zu desinfizierenden System oder auf der zu desinfizierenden Oberfläche verbleiben und nicht ausgespült werden.Disinfectants in use. Preparations based on peroxidic active ingredients, in particular peracetic acid, on the other hand, have gained little importance for this application. An important reason is the low storage stability of such aqueous preparations. Because of the broad antimicrobial effectiveness of the peroxides, there has been no shortage of attempts to overcome the disadvantage of the poor storage stability. For example, it has been proposed in German Offenlegungsschriften 26 55 599 and 28 15 400 that the aqueous preparations required for disinfection be prepared shortly before use from more stable precursors, namely from sodium perborate and acid anhydrides. According to German Offenlegungsschrift 27 01 133, the aqueous preparations are obtained from hydrogen peroxide releasers and aromatic acyloxycarboxylic acids. However, only a few of these compounds provide disinfectant solutions with a sufficiently broad activity, and the storage of these acylating agents in a mixture with the necessary inorganic peroxides is only possible for a limited time because of the decomposition reactions. Under the name Sekusept powder is a product on the market, when it is dissolved in water by reacting sodium perborate with tetraacetylethyl lendiamine (TAED) is a disinfectant preparation. This product based on an N-acyl compound has a broad spectrum of activity and is stable in storage. Although a high standard has already been achieved in the disinfection of medical instruments in this way, efforts have been made to improve the peroxidic systems in order to eliminate any gaps in use and disadvantages in use. A particular disadvantage of such powdery systems is that they dissolve very slowly in water. On the one hand, this results in the disadvantage that the desired disinfectant concentration is only fully available very late. On the other hand, there is also the risk that undissolved components remain in the system to be disinfected or on the surface to be disinfected and are not rinsed out.
Aufgabe der vorliegenden Erfindung war es daher, innerhalb kurzer Zeit eine ausreichende Desinfektionsmittelkonzentration zur Verfügung zu stellen und dabei das Risiko von Rückständen im System und auf den Oberflächen gering zu halten.The object of the present invention was therefore to provide a sufficient disinfectant concentration within a short time and to keep the risk of residues in the system and on the surfaces low.
Es sollte auch erreicht werden, innerhalb kürzerer Zeit die Abtötung von Mikroorganismen, auch von Mykobakterien zu erreichen.It should also be achieved to kill microorganisms, including mycobacteria, within a shorter period of time.
Diese Aufgabe wurde gelöst durch die erfindungsgemäßen Mittel.This object was achieved by the means according to the invention.
Dementsprechend ist Gegenstand der vorliegenden Erfindung ein pulverförmiges Desinfektionsmittel auf Aktivsauerstoffbasis, enthaltend ein Peressigsäure generierendes System aus einem Peroxid und einem Acylierungsmittel zusammen mit nichtionischen Tensiden.Accordingly, the present invention relates to a powdery disinfectant based on active oxygen, containing a peracetic acid-generating system consisting of a peroxide and an acylating agent together with nonionic surfactants.
Vorzugsweise sind dabei die genannten nichtionischen Tenside frei von alkoxylierten Alkylphenolen und umfassen geradkettige oder in 2-Stellung methylverzweigte Etheralkohole der FormelThe nonionic surfactants mentioned are preferably free from alkoxylated alkylphenols and include straight-chain or ether alcohols of the formula which are methyl-branched in the 2-position
R-0-(PO)ι.2-(EO)6-8-H (I) wobei die Alkyl- bzw. Alkenylreste R wie folgt zusammengesetzt sind: C8 = 0-5 Gew.%; C9-10 = 75-90 Gew.%; Cn-ι2 = 5-15 Gew.%; C13-14 = 4-10 Gew.%; C15-16 = 0-3 Gew.%.R-0- (PO) ι. 2 - (EO) 6 -8-H (I) where the alkyl or alkenyl radicals R are composed as follows: C 8 = 0-5% by weight; C 9 - 10% by weight = 75-90;. Cn-ι 2 = 5-15% by weight; C 13-14 = 4-10% by weight; C 15-16 = 0-3% by weight.
Das genannte Peroxid ist vorzugsweise ausgewählt aus der Gruppe Natriumperboratmonohydrat, Natriumperborattetrahydrat, Natriumpercarbonat und deren Mischungen.Said peroxide is preferably selected from the group sodium perborate monohydrate, sodium perborate tetrahydrate, sodium percarbonate and mixtures thereof.
Das genannte Acylierungsmittel ist vorzugsweise ausgewählt aus der Gruppe Tetraacetylglykoluril, Tetraacetylethylendiamin, Diacetylhexahydrotriazindion und deren Mischungen.The acylating agent mentioned is preferably selected from the group tetraacetylglycoluril, tetraacetylethylenediamine, diacetylhexahydrotriazinedione and mixtures thereof.
Selbstverständlich können auch andere N-Acylverbindungen in Frage kommen, die auch im Bereich der Waschmittelchemie als sogenannte Bleichaktivatoren zur Umsetzung mit Wasserstoffperoxid in alkalischen Waschflotten beschrieben worden sind. Geeignete N-Acylverbindungen sind insbesondere diejenigen, die an dem Stickstoff, der die Acylgruppe trägt, eine weitere Ketogruppe aufweisen, und/oder in denen der Stickstoff Teil eines heterocyclischen Ringsystems ist. Beispiele geeigneter N-Acylverbindungen sind die mehrfach acylierten Alkylendiamine, wie etwa Tetraacetylethylendiamin, acylierte Glykolurile, in erster Linie Tetraacetylglykoluril, N-acylierte Hydantoine, Hydrazide, Triazole, Triazine, Urazole, Diketopiperazine, Sulfurylamide, Lactame und Cyanurate.Of course, other N-acyl compounds can also be used, which have also been described in the field of detergent chemistry as so-called bleach activators for reaction with hydrogen peroxide in alkaline washing liquors. Suitable N-acyl compounds are in particular those which have a further keto group on the nitrogen which carries the acyl group and / or in which the nitrogen is part of a heterocyclic ring system. Examples of suitable N-acyl compounds are the multiply acylated alkylenediamines, such as tetraacetylethylenediamine, acylated glycolurils, primarily tetraacetylglycoluril, N-acylated hydantoins, hydrazides, triazoles, triazines, urazoles, diketopiperazines, sulfurylamides, lactams and cyanurates.
Vorzugsweise enthält das erfindungsgemäße DesinfektionsmittelThe disinfectant according to the invention preferably contains
10 bis 70 Gew.-%, vorzugsweise 15 bis 60 Gew.-% des genannten10 to 70 wt .-%, preferably 15 to 60 wt .-% of the above
Peroxids,peroxide,
10 bis 40 Gew.-%, vorzugsweise 15 bis 30 Gew.-% des genannten10 to 40 wt .-%, preferably 15 to 30 wt .-% of the above
Acylierungsmittels,acylating agent,
0,1 bis 10 Gew.-%, vorzugsweise 0,5 bis 5 Gew.-% des genannten nichtionischen Tensids und als Rest auf 100 Gew.-% lösliches anorganisches Salz und ggf. weitere Hilfsstoffe.0.1 to 10 wt .-%, preferably 0.5 to 5 wt .-% of said nonionic surfactant and the remainder to 100% by weight of soluble inorganic salt and possibly other auxiliaries.
Als weitere Hilfsstoffe kommen Alkalisierungsmittel, Komplexbildner für Wasserhärte, Komplexbildner für Schwermetallionen und wasserlösliche anorganische Salze, Korrosionsinhibitoren und andere Tenside in Betracht. Die Menge an derartigen Hilfsstoffen kann in den Zubereitungen in sehr weiten Grenzen, abhängig von der beabsichtigten Wirkung, schwanken. Sie liegt üblicherweise nicht über etwa 3 Gew.-%, vorzugsweise zwischen etwa 0,001 und etwa 1 Gew.- %, bezogen auf die gesamte ZubereitungAlkalizing agents, complexing agents for water hardness, complexing agents for heavy metal ions and water-soluble inorganic salts, corrosion inhibitors and other surfactants are also suitable as auxiliary agents. The amount of such auxiliaries in the preparations can vary within very wide limits, depending on the intended effect. It is usually not more than about 3% by weight, preferably between about 0.001 and about 1% by weight, based on the overall preparation
Als Komplexbildner für die Wasserhärte ist in erster Linie Natriumtriphosphat zu erwähnen, doch kommen hierfür auch andere Polyphosphate, Salze der Nitrilotriessigsäure und Salze von organischen Polycarbonsäuren, beispielsweise Citronensäure, oder von polymeren Polycarbonsäuren, beispielsweise Acrylsäure- Maleinsäure-Copolymerisaten, in Betracht. Besonders bevorzugt wird Natriumtriphosphat, das zugleich als Alkalisierungsmittel wirkt.Sodium triphosphate is to be mentioned primarily as a complexing agent for the water hardness, but other polyphosphates, salts of nitrilotriacetic acid and salts of organic polycarboxylic acids, for example citric acid, or of polymeric polycarboxylic acids, for example acrylic acid / maleic acid copolymers, are also suitable for this purpose. Sodium triphosphate, which also acts as an alkalizing agent, is particularly preferred.
Als Komplexbildner für Schwermetallionen, die zersetzend auf peroxidische Verbindungen wirken, kommen in erster Linie Aminopolycarbonsäuren bzw. deren Salze, beispielsweise Ethylendiamintetraessigsäure, insbesondere aber Aminopolyphosphonsäuren, wie Ethylendiamintetramethylenphosphonsäure, oder auch Hydroxyethandiphosphonsäure bzw. deren Salze in Betracht.Suitable complexing agents for heavy metal ions, which have a decomposing effect on peroxidic compounds, are primarily aminopolycarboxylic acids or their salts, for example ethylenediaminetetraacetic acid, but in particular aminopolyphosphonic acids, such as ethylenediaminetetramethylenephosphonic acid, or else hydroxyethane diphosphonic acid or salts thereof.
Wasserlösliche Salze können die Funktion von Füllstoffen oder Gerüststoffen übernehmen, wie beispielsweise Natriumsulfat, sofern sie nicht gleichzeitig alkalisierende Wirkung haben, wie beispielsweise Natriumcarbonat und Natriumsilikat. Als Korrosionsinhibitoren sind insbesondere Alkylphosphonsäuren zu erwähnen, von denen Octanphosphonsäure besonders bevorzugt wird. Als weitere mögliche Hilfsstoffe sind Farbstoffe, Parfüm und lösungsvermittelnde Zusätze zu erwähnen. Bei der Anwendung wird das Desinfektionsmittel in üblicher weise mit Wasser verdünnt.Water-soluble salts can take on the function of fillers or builders, such as sodium sulfate, provided that they do not simultaneously have an alkalizing effect, such as sodium carbonate and sodium silicate. Corrosion inhibitors which should be mentioned are, in particular, alkylphosphonic acids, of which octanephosphonic acid is particularly preferred. Dyes, perfume and solubilizing additives should be mentioned as further possible auxiliaries. When used, the disinfectant is usually diluted with water.
Es wird vorzugsweise in einer Menge von 1 bis 10 Gew.-% in Wasser gelöst.It is preferably dissolved in water in an amount of 1 to 10% by weight.
In einer bevorzugten Ausführungsform wird das erfindungsgemäße Desinfektionsmitteln für die Oberflächendesinfektion und/oderIn a preferred embodiment, the disinfectant according to the invention for surface disinfection and / or
Instrumentendesinfektion verwendet.Instrument disinfection used.
Außerdem ist es bevorzugt, das erfindungsgemäße Desinfektionsmitteln zur Abtötung von grampositiven Bakterien, und/oder zur Abtötung von Mykobakterien und/oder zur Abtötung von Viren zu verwenden. In addition, it is preferred to use the disinfectant according to the invention to kill gram-positive bacteria and / or to kill mycobacteria and / or to kill viruses.
B e i s p i e l eB e i s p i e l e
1. Herstellung der Wirkstofflösung1. Preparation of the active ingredient solution
Es wurde ausgegangen von drei unterschiedlichen pulverförmigen Gemischen, jeweils bestehend ausIt was assumed that three different powdery mixtures, each consisting of
50 Gew.-% Natriumperboratmonohydrat und 25 Gew.-% TAED-Pulver sowie a) kein Tensid b) 2 Gew.% ABS (Alkylbenzolsulfonat) und c) 2 Gew.% Dehydol 98050% by weight sodium perborate monohydrate and 25% by weight TAED powder and a) no surfactant b) 2% by weight ABS (alkylbenzenesulfonate) and c) 2% by weight dehydol 980
Dabei wurden als Rest auf 100 Gew.% Korrosionsinhibitoren, Komplexbildner und weitere anorganische Salze eingesetzt.Corrosion inhibitors, complexing agents and other inorganic salts were used as the remainder to 100% by weight.
In einem ersten Versuch wurde das Auflöseverhalten dieser unterschiedlichen Pulver-Formulierungen 1a) bis 1c) in Wasser ohne Rühren oder sonstige Bewegung untersucht.In a first experiment, the dissolution behavior of these different powder formulations 1a) to 1c) in water without stirring or other movement was examined.
Hierfür wurden je 8 g der Pulver-Formulierungen 1a) bis 1c) in je 100 ml Leitungswasser bei Raumtemperatur gegeben.For this purpose, 8 g of powder formulations 1a) to 1c) were placed in 100 ml of tap water at room temperature.
Dabei zeigte sich, daß der Zeitaufwand, der zur Auflösung der Formulierungen 1a) und 1b) erforderlich war, über eine Stunde betrug. Hinzu kam, daß sich bei der Pulver-Formulierung 1b) außerdem ein Bodensatz bildete.It was found that the time required to dissolve formulations 1a) and 1b) was over an hour. In addition, a sediment was also formed in powder formulation 1b).
Bei der Pulver-Formulierung 1c) hingegen war das Pulver innerhalb einer Stunde gelöst. Es bildete sich außerdem kein Bodensatz.In contrast, with powder formulation 1c), the powder was dissolved within one hour. In addition, no sediment was formed.
Zur Erklärung:For explanation:
Dehydol 980 ist ein in 2-Stellung methylverzweigter Etheralkohol der FormelDehydol 980 is a 2-position methyl branched ether alcohol of the formula
R-0-(PO)1.2-(EO)6-8-H (I) wobei die Alkyl- bzw. Alkenylreste R wie folgt zusammengesetzt sind:R-0- (PO) 1 . 2 - (EO) 6-8 -H (I) where the alkyl or alkenyl radicals R are composed as follows:
C8 = 0-5 Gew.%; C9-ιo = 75-90 Gew.%; Cn.ι2 = 5-15 Gew.%;C 8 = 0-5% by weight; C = 9- ιo 75-90% wt. Cn.ι 2 = 5-15% by weight;
2. Prüfung der Wirksamkeit gegen das grampositive Bakterium Enterococcus hirae2. Testing the effectiveness against the gram-positive Enterococcus hirae bacterium
Mit den Pulver-Formulierungen 1a) und 1c) wurden durch Lösen von je 12,5 g in je 100 ml Leitungswasser Anwendungslösungen für mikrobiologischen Untersuchungen angesetzt.With powder formulations 1a) and 1c), application solutions for microbiological tests were prepared by dissolving 12.5 g each in 100 ml tap water.
Diese Lösungen wurden im quantitativen Keimträgertest nach neuer DGHM Richtlinie unter organischer Belastung ("dirty conditions") (Stand 1.3.2001) gegen das grampositive Bakterium Enterococcus hirae geprüft. Dabei wurden folgende log-Reduktionsfaktoren (jeweils Dreifachbestimmung) ermittelt:These solutions were tested in a quantitative germ carrier test according to the new DGHM guideline under organic pollution ("dirty conditions") (status 1.3.2001) against the gram-positive bacterium Enterococcus hirae. The following log reduction factors (triple determination) were determined:
Einwirkzeit 1c) 1a)Exposure time 1c) 1a)
1 min 3,06/2,23/3,1 0,53/0,61/0,481 min 3.06 / 2.23 / 3.1 0.53 / 0.61 / 0.48
5 min 3,22/3,81/2,98 1 ,74/1 ,41/1 ,335 min 3.22 / 3.81 / 2.98 1, 74/1, 41/1, 33
10 min 6,8/6,8/6,8 3,72/3,46/3,810 min 6.8 / 6.8 / 6.8 3.72 / 3.46 / 3.8
Auch bezüglich der antimikrobiellen Wirksamkeit ist somit ein deutlicher Vorteil der erfindungsgemäßen Formulierungen erkennbar.A clear advantage of the formulations according to the invention can also be seen in terms of the antimicrobial activity.
3. Prüfung der Wirksamkeit gegen Poliovirus3. Testing effectiveness against poliovirus
Mit den Pulver-Formulierungen 1a) und 1c) wurden durch Lösen von je 12,5 g in je 100 ml Leitungswasser Anwendungslösungen für mikrobiologischen Untersuchungen angesetzt. Diese Lösungen wurden im quantitativen Suspensionstes nach DW Richtlinie gegen Poliovirus geprüft. Dabei wurden folgende durchschnittliche log- Reduktionsfaktoren (jeweils Dreifachbestimmung) ermittelt:With the powder formulations 1a) and 1c), application solutions for microbiological tests were prepared by dissolving 12.5 g each in 100 ml tap water. These solutions were tested in quantitative suspension tests according to DW guidelines against poliovirus. The following average log reduction factors (triple determination) were determined:
Einwirkzeit 1c) 1a)Exposure time 1c) 1a)
5 min 1 ,5 1 ,55 min 1, 5 1, 5
10 min 3,3 2,610 min 3.3 2.6
Auch die virologischen Prüfergebnisse lassen somit einen Vorteil erkennen. The virological test results also show an advantage.
Claims
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE50311661T DE50311661D1 (en) | 2002-04-03 | 2003-03-25 | INSTRUMENT END INFECTION |
| EP03722354A EP1489908B1 (en) | 2002-04-03 | 2003-03-25 | Disinfection of instruments |
| HU0500441A HUP0500441A3 (en) | 2002-04-03 | 2003-03-25 | Disinfection of instruments |
| US10/509,806 US20050153854A1 (en) | 2002-04-03 | 2003-03-25 | Disinfection of instruments |
| US11/859,036 US20080014284A1 (en) | 2002-04-03 | 2007-09-21 | Disinfection of instruments |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10214750A DE10214750A1 (en) | 2002-04-03 | 2002-04-03 | Instrument disinfection |
| DE10214750.7 | 2002-04-03 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/859,036 Continuation US20080014284A1 (en) | 2002-04-03 | 2007-09-21 | Disinfection of instruments |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2003082014A1 true WO2003082014A1 (en) | 2003-10-09 |
Family
ID=28051074
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2003/003065 Ceased WO2003082014A1 (en) | 2002-04-03 | 2003-03-25 | Disinfection of instruments |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US20050153854A1 (en) |
| EP (1) | EP1489908B1 (en) |
| DE (2) | DE10214750A1 (en) |
| ES (1) | ES2326370T3 (en) |
| HU (1) | HUP0500441A3 (en) |
| PL (1) | PL211269B1 (en) |
| WO (1) | WO2003082014A1 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010102188A1 (en) * | 2009-03-05 | 2010-09-10 | E. I. Du Pont De Nemours And Company | Multi-part kit system for the preparation of a disinfectant of the peracetic acid type |
| EP2692844A1 (en) * | 2012-08-01 | 2014-02-05 | Chemische Fabrik Dr. Weigert GmbH & Co KG | Cleaner and disinfectant for medical instruments |
| US8958881B2 (en) | 2005-08-19 | 2015-02-17 | Brainsgate Ltd. | Neuroprotective electrical stimulation |
| WO2025099168A1 (en) * | 2023-11-07 | 2025-05-15 | Eberhard Karls Universität Tübingen | Storable multi-component compositions comprising a stable biocide component |
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| US7470655B2 (en) * | 2004-08-06 | 2008-12-30 | Ecolab Inc. | Method of inactivating prions |
| US9700644B2 (en) * | 2006-08-15 | 2017-07-11 | American Sterilizer Company | One part, solids containing decontamination blend composition |
| US9724550B2 (en) * | 2006-08-15 | 2017-08-08 | American Sterilizer Company | One part, solids containing decontamination blend composition |
| US20100075883A1 (en) * | 2008-09-24 | 2010-03-25 | Ecolab Inc. | Granular cleaning and disinfecting composition |
| GB201010374D0 (en) * | 2010-06-21 | 2010-08-04 | Mtp Innovations Ltd | Disinfectant composition |
| CA2759344C (en) | 2011-08-31 | 2016-10-11 | DeVere Company, Inc. | Antimicrobial surface treatment composition comprising a peroxygen compound, a chlorinated isocyanurate salt, and a bleach activator |
| US20140308162A1 (en) | 2013-04-15 | 2014-10-16 | Ecolab Usa Inc. | Peroxycarboxylic acid based sanitizing rinse additives for use in ware washing |
| US9994799B2 (en) | 2012-09-13 | 2018-06-12 | Ecolab Usa Inc. | Hard surface cleaning compositions comprising phosphinosuccinic acid adducts and methods of use |
| US8871699B2 (en) | 2012-09-13 | 2014-10-28 | Ecolab Usa Inc. | Detergent composition comprising phosphinosuccinic acid adducts and methods of use |
| US9752105B2 (en) | 2012-09-13 | 2017-09-05 | Ecolab Usa Inc. | Two step method of cleaning, sanitizing, and rinsing a surface |
| US10426854B2 (en) | 2016-09-28 | 2019-10-01 | Medivators Inc. | Apparatus and method to make high level disinfectant |
| CN111575118B (en) | 2016-10-18 | 2022-10-28 | 斯特里莱克斯有限责任公司 | Ambient moisture activatable surface treatment powders |
| CN109392903B (en) * | 2018-11-02 | 2021-04-06 | 广东环凯微生物科技有限公司 | Peroxycarboxylic acid disinfectant and preparation method thereof |
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- 2003-03-25 EP EP03722354A patent/EP1489908B1/en not_active Expired - Lifetime
- 2003-03-25 US US10/509,806 patent/US20050153854A1/en not_active Abandoned
- 2003-03-25 ES ES03722354T patent/ES2326370T3/en not_active Expired - Lifetime
- 2003-03-25 PL PL371013A patent/PL211269B1/en unknown
- 2003-03-25 HU HU0500441A patent/HUP0500441A3/en unknown
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| US8958881B2 (en) | 2005-08-19 | 2015-02-17 | Brainsgate Ltd. | Neuroprotective electrical stimulation |
| WO2010102188A1 (en) * | 2009-03-05 | 2010-09-10 | E. I. Du Pont De Nemours And Company | Multi-part kit system for the preparation of a disinfectant of the peracetic acid type |
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| WO2025099168A1 (en) * | 2023-11-07 | 2025-05-15 | Eberhard Karls Universität Tübingen | Storable multi-component compositions comprising a stable biocide component |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1489908A1 (en) | 2004-12-29 |
| HUP0500441A3 (en) | 2009-05-28 |
| PL371013A1 (en) | 2005-06-13 |
| DE50311661D1 (en) | 2009-08-13 |
| US20050153854A1 (en) | 2005-07-14 |
| US20080014284A1 (en) | 2008-01-17 |
| ES2326370T3 (en) | 2009-10-08 |
| DE10214750A1 (en) | 2003-10-16 |
| EP1489908B1 (en) | 2009-07-01 |
| PL211269B1 (en) | 2012-04-30 |
| HUP0500441A2 (en) | 2006-04-28 |
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